Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yu. A. Kondrova"'
Autor:
Yu. A. Kondrova, M. G. Safarov, V. S. Kolosnitsyn, Farid A. Valeev, L. Kh. Faizullina, Leonid V. Spirikhin
Publikováno v:
Russian Journal of Organic Chemistry. 47:914-919
Michael reactions of levoglucosenone and its α-bromo and α-iodo derivatives with α,ω-dinitroalkanes were studied under conditions of chemical and electrochemical generation of base. Procedures were developed for stereospecific fusion of a cyclope
Publikováno v:
Russian Journal of Organic Chemistry. 46:1151-1156
The Diels-Alder adduct of levoglucosenone and piperylene was converted into the corresponding oxime, and second-order Beckmann rearrangement of the latter, followed by treatment with a base, gave (1S,2R,6R)-6-(2-hydroxyethyl)-2-methylcyclohex-3-ene-1
Autor:
V. S. Kolosnitsyn, L. Kh. Faizullina, Leonid V. Spirikhin, Farid A. Valeev, M. G. Safarov, Yu. A. Kondrova
Publikováno v:
ChemInform. 42
Michael reactions of levoglucosenone (VI) and its halo derivatives (I) with α,ω-dinitroalkanes are examined under conditions of chemical and electrochemical generation of base.
Publikováno v:
ChemInform. 42
The Diels-Alder adduct (I) of levoglucosenone and piperylene is used as starting compound for the synthesis of aldehyde (VII), a building block for the synthesis of eleutheside analogues.